• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

缓激肽B2受体拮抗剂NPC - 567对猪模型中变应原诱导的气道反应的影响。

The effect of a bradykinin B2 receptor antagonist, NPC-567, on allergen-induced airway responses in a porcine model.

作者信息

Sylvin H, van der Ploeg I, Alving K

机构信息

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Inflamm Res. 2001 Sep;50(9):453-9. doi: 10.1007/PL00000270.

DOI:10.1007/PL00000270
PMID:11603850
Abstract

OBJECTIVE AND DESIGN

In order to assess the effect of selective blocking of the bradykinin (BK) B2 receptor in allergic airway reactions, the BK B2 receptor antagonist NPC-567 was administered to sensitized pigs before allergen challenge.

MATERIAL

Fourteen specific pathogen-free pigs sensitized to Ascaris suum were used.

TREATMENT

NPC-567 (2.5 mg, in 1 ml saline) was delivered as an aerosol twice to six pigs.

METHODS

Ascaris antigen (in 2 ml saline) was given as an aerosol to all pigs and airway mechanics were monitored for 8 h. NPC-567 (2.5 mg) was given at t = -30 min (in 1ml saline) and mixed with the antigen at t = 0 to six pigs.

RESULTS

Allergen challenge caused an acute reaction with a rapid, significant increase in airways resistance from 4.1 +/- 0.5 cm H2O/l/s to a maximum of 16.2 +/- 3.0 cm H2O/l/s in the control pigs. In the NPC-567-treated pigs, the resistance only increased from 2.9 +/- 0.3 cm H2O/l/s to 6.5 +/- 0.9 cm H2O/l/s (p<0.005 compared to controls). There was also a higher reduction in dynamic lung compliance in the controls than in the treated animals upon allergen challenge. The histamine concentration in urine in the control pigs was markedly elevated after allergen challenge peaking at 15-30 min. This release was inhibited in the NPC-567-treated pigs.

CONCLUSIONS

The BK B2 receptor antagonist NPC-567 seems to be effective in inhibiting the acute response to allergen in the pig airways, possibly due to inhibition of mast cell activation via indirect mechanisms. The late obstructive response was reduced as well, probably as a consequence of the reduced mediator release in the acute reaction.

摘要

目的与设计

为了评估缓激肽(BK)B2受体选择性阻断在过敏性气道反应中的作用,在变应原激发前,将BK B2受体拮抗剂NPC - 567给予致敏猪。

材料

使用14头对猪蛔虫致敏的无特定病原体猪。

处理

将NPC - 567(2.5毫克,溶于1毫升生理盐水)以气雾剂形式分两次给予6头猪。

方法

将猪蛔虫抗原(溶于2毫升生理盐水)以气雾剂形式给予所有猪,并监测气道力学8小时。在t = - 30分钟时,将NPC - 567(2.5毫克)(溶于1毫升生理盐水)给予6头猪,并在t = 0时与抗原混合。

结果

变应原激发引起急性反应,对照猪的气道阻力从4.1±0.5厘米水柱/升/秒迅速显著增加至最高16.2±3.0厘米水柱/升/秒。在接受NPC - 567治疗的猪中,阻力仅从2.9±0.3厘米水柱/升/秒增加至6.5±0.9厘米水柱/升/秒(与对照组相比,p < 0.005)。变应原激发后,对照猪的动态肺顺应性降低幅度也高于治疗组动物。变应原激发后,对照猪尿液中的组胺浓度在15 - 30分钟达到峰值时显著升高。在接受NPC - 567治疗的猪中,这种释放受到抑制。

结论

BK B2受体拮抗剂NPC - 567似乎能有效抑制猪气道对变应原的急性反应,这可能是由于通过间接机制抑制了肥大细胞的激活。迟发性阻塞反应也有所减轻,这可能是急性反应中介质释放减少的结果。

相似文献

1
The effect of a bradykinin B2 receptor antagonist, NPC-567, on allergen-induced airway responses in a porcine model.缓激肽B2受体拮抗剂NPC - 567对猪模型中变应原诱导的气道反应的影响。
Inflamm Res. 2001 Sep;50(9):453-9. doi: 10.1007/PL00000270.
2
A bradykinin antagonist modifies allergen-induced mediator release and late bronchial responses in sheep.一种缓激肽拮抗剂可改变绵羊体内变应原诱导的介质释放和迟发性支气管反应。
Am Rev Respir Dis. 1991 Apr;143(4 Pt 1):787-96. doi: 10.1164/ajrccm/143.4_Pt_1.787.
3
The tryptase inhibitor APC-366 reduces the acute airway response to allergen in pigs sensitized to Ascaris suum.类胰蛋白酶抑制剂APC-366可降低对猪蛔虫致敏的猪对过敏原的急性气道反应。
Clin Exp Allergy. 2002 Jun;32(6):967-71. doi: 10.1046/j.1365-2222.2002.01239.x.
4
Effects of bradykinin receptor antagonists on antigen-induced respiratory distress, airway hyperresponsiveness and eosinophilia in guinea-pigs.缓激肽受体拮抗剂对豚鼠抗原诱导的呼吸窘迫、气道高反应性和嗜酸性粒细胞增多的影响。
Br J Pharmacol. 1992 Nov;107(3):653-9. doi: 10.1111/j.1476-5381.1992.tb14502.x.
5
Selective protective effects of nitric oxide inhalation on allergen-induced acute airway reactions in the pig.一氧化氮吸入对猪变应原诱导的急性气道反应的选择性保护作用。
Clin Exp Allergy. 2001 Nov;31(11):1787-95. doi: 10.1046/j.1365-2222.2001.01227.x.
6
Inhibitory effect of NPC-17731 on BK-induced and antigen-induced airway reactions in guinea-pigs.NPC-17731对豚鼠BK诱导和抗原诱导的气道反应的抑制作用。
Clin Exp Allergy. 1998 May;28(5):635-43. doi: 10.1046/j.1365-2222.1998.00264.x.
7
Effects of local and systemic budesonide on allergen-induced airway reactions in the pig.局部和全身应用布地奈德对猪变应原诱导的气道反应的影响。
Br J Pharmacol. 1996 Jun;118(4):989-97. doi: 10.1111/j.1476-5381.1996.tb15497.x.
8
The interaction of alpha 1-proteinase inhibitor and tissue kallikrein in controlling allergic ovine airway hyperresponsiveness.α1-蛋白酶抑制剂与组织激肽释放酶在控制绵羊过敏性气道高反应性中的相互作用。
Am J Respir Crit Care Med. 1996 Jul;154(1):36-42. doi: 10.1164/ajrccm.154.1.8680696.
9
Effect of nedocromil sodium on allergen-, PAF-, histamine- and bradykinin-induced airways vasodilatation and pulmonary obstruction in the pig.奈多罗米钠对猪体内变应原、血小板活化因子、组胺及缓激肽诱导的气道血管舒张和肺阻塞的影响。
Br J Pharmacol. 1991 Oct;104(2):452-8. doi: 10.1111/j.1476-5381.1991.tb12450.x.
10
Suppressive effect of distinct bradykinin B2 receptor antagonist on allergen-evoked exudation and leukocyte infiltration in sensitized rats.不同缓激肽B2受体拮抗剂对致敏大鼠变应原诱发的渗出和白细胞浸润的抑制作用。
Br J Pharmacol. 1999 May;127(2):315-20. doi: 10.1038/sj.bjp.0702536.

引用本文的文献

1
Kininogen deficiency or depletion reduces enhanced pause independent of pulmonary inflammation in a house dust mite-induced murine asthma model.激肽原缺乏或耗竭可减少屋尘螨诱导的小鼠哮喘模型中增强的呼吸暂停,而不依赖于肺部炎症。
Am J Physiol Lung Cell Mol Physiol. 2019 Jan 1;316(1):L187-L196. doi: 10.1152/ajplung.00162.2018. Epub 2018 Oct 25.
2
Localized Th1-, Th2-, T regulatory cell-, and inflammation-associated hepatic and pulmonary immune responses in Ascaris suum-infected swine are increased by retinoic acid.猪蛔虫感染猪中,视黄酸可增强局部Th1、Th2、调节性T细胞以及与炎症相关的肝脏和肺部免疫反应。
Infect Immun. 2009 Jun;77(6):2576-87. doi: 10.1128/IAI.00827-07. Epub 2009 Mar 30.
3
The Quintiles Prize Lecture 2004. The identification of the adenosine A2B receptor as a novel therapeutic target in asthma.
2004年昆泰奖讲座。腺苷A2B受体作为哮喘新治疗靶点的鉴定。
Br J Pharmacol. 2005 Aug;145(8):1009-15. doi: 10.1038/sj.bjp.0706272.